C2750732[trait identifier] AND "3billion"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1320232	NM_002524.5(NRAS):c.449A>G (p.Gln150Arg)	NRAS (Q150R)	Single nucleotide variant (missense variant)	Noonan syndrome 6	GLikely pathogenic
Select item 40469	NM_002524.5(NRAS):c.34G>C (p.Gly12Arg)	NRAS (G12R)	Single nucleotide variant (missense variant)	Noonan syndrome 6 +2 more	GPathogenic